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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 86711990、化合物

HRID 1051348
ノート
印刷プレビュー

反応式

HRID 1051348 の反応式
[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([C:11]([OH:13])=O)[NH:6]2.[NH4+].[Cl-].CC[N:18]=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1>CN(C=O)C>[F:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([C:11]([NH2:18])=[O:13])[NH:6]2
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 25517Ammonium ChlorideHCID 757711-HydroxybenzotriazoleHCID 40355794-Fluoroindole-2-carboxylic acid

生成物 1

HCID 86711990HCID 86711990、化合物収率 73%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

To a solution of 34 (179 mg, 1.00 mmol) in anhydrous DMF (2.0 mL) were added NH4Cl (160 mg, 3.00 mmol), EDCI (395 mg, 2.20 mmol), HOBt (297 mg, 2.20 mmol) and TEA (303 mg, 3.00 mmol) at RT. After stirring at RT for 3 h, the mixture was quenched with H2O (10 mL) the resulting mixture was extracted with EtOAc (3×6 mL). The combined extracts were dried and concentrated. The residue was purified by SiO2 chromatography eluting with petroleum ether/EtOAc (5:1 to 3:1) to afford 130 mg (73%) of 4-fluoro-1H-indole-2-carboxamide (36) as a white solid. LCMS (ESI) m/z: 179.1 [M+H]+.

後処理

  1. customthe mixture was quenched with H2O (10 mL) the resulting mixture
  2. extractionwas extracted with EtOAc (3×6 mL)
  3. customThe combined extracts were dried
  4. concentrationconcentrated
  5. customThe residue was purified by SiO2 chromatography
  6. washeluting with petroleum ether/EtOAc (5:1 to 3:1)

出典と根拠

ORDレコード
ord-5f4fe5ce8bac4441bbaaf4967605efe4
出典データセット
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09388171B2

反応ノート

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